Status and phase
Conditions
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Study type
Funder types
Identifiers
About
This study will assess the safety and preliminary efficacy of escalating doses of LGH447 monotherapy in AML and MDS and LGH447 in combination with midostaurin in AML.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion Criteria
-Male or female patients ≥18 years of age who present with one of the following:
LGH447 monotherapy arm
LGH447 and midostaurin combination arm
Refractory/Relapsed AML following no more than 2 prior therapies, or in previously untreated AML patients who are not candidates for standard therapy. AML patients may have either FLT3 wild type or FLT3-ITD/TKD mutant disease, and FLT3 mutation status needs to be defined at study entry.
Platelet count > 25,000/mm3
Neutrophils > 500/mm3
Blood transfusions are allowed to maintain clinically adequate hemoglobin and hematocrit levels
Exclusion Criteria
Primary purpose
Allocation
Interventional model
Masking
70 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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